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Completed Phase 3 Interventional Results available

Clinical Study of Cefiderocol (S-649266) for the Treatment of Nosocomial Pneumonia Caused by Gram-negative Pathogens

ClinicalTrials.gov ID: NCT03032380

Public ClinicalTrials.gov record NCT03032380. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 1:40 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Parallel-group, Clinical Study of S-649266 Compared With Meropenem for the Treatment of Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacterial Pneumonia, or Healthcare-associated Bacterial Pneumonia Caused by Gram-negative Pathogens

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to compare all-cause mortality at Day 14 in participants receiving cefiderocol with participants receiving the comparator, meropenem, in adults with hospital-acquired bacterial pneumonia (HABP), ventilator-associated bacterial pneumonia (VABP), or healthcare-associated bacterial pneumonia (HCABP) caused by Gram-negative pathogens.

Study identification

NCT ID
NCT03032380
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Shionogi
Industry
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 24, 2017 (Actual)
Primary completion
Feb 26, 2019 (Actual)
Completion
Apr 1, 2019 (Actual)
Last update posted
Nov 13, 2020

2017 – 2019

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Shionogi Research Site New Haven Connecticut 06511 —
Shionogi Research Site DeLand Florida 32720 —
Shionogi Research Site Chicago Illinois 60612 —
Shionogi Research Site Council Bluffs Iowa 51503 —
Shionogi Research Site Louisville Kentucky 40202 —
Shionogi Research Site Baton Rouge Louisiana 70808 —
Shionogi Research Site Shreveport Louisiana 71103 —
Shionogi Research Site Annapolis Maryland 21404 —
Shionogi Research Site Detroit Michigan 48201 —
Shionogi Research Site St Louis Missouri 63110-0250 —
Shionogi Research Site Cleveland Ohio 44106 —
Shionogi Research Site Columbus Ohio 43210-1267 —
Shionogi Research Site Bethlehem Pennsylvania 18105 —
Shionogi Research Site Philadelphia Pennsylvania 19141 —
Shionogi Research Site Salt Lake City Utah 84132 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03032380, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 13, 2020 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03032380 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →